CN102872149B - Application of Houttuynoid B in medicament for treating cecum cancer - Google Patents

Application of Houttuynoid B in medicament for treating cecum cancer Download PDF

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CN102872149B
CN102872149B CN 201210419692 CN201210419692A CN102872149B CN 102872149 B CN102872149 B CN 102872149B CN 201210419692 CN201210419692 CN 201210419692 CN 201210419692 A CN201210419692 A CN 201210419692A CN 102872149 B CN102872149 B CN 102872149B
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houttuynoid
application
cecum cancer
treating
medicament
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CN102872149A (en
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宋海平
刘德亮
孙晶
黄晨
吴俊艺
吴俊华
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Song Haiping
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宋海平
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Abstract

The invention discloses an application of Houttuynoid B in a medicament for treating cecum cancer, and belongs to the technical field of new application of medicaments. In-vitro methyl thiazolyl tetrazolium (MTT) anti-tumor activity evaluation shows that the Houttuynoid B has a remarkable inhibiting effect on growth of a human cecum cancer cell line HCT-8. Therefore, the Houttuynoid B can be usedfor preparing the cecum cancer resistant medicament, and has a good development and application prospect. The invention discloses the application of the Houttuynoid B in preparation of the medicamentfor treating the cecum cancer for the first time, the skeleton type belongs to a brand-new skeleton type, and the Houttuynoid B has unexpected strong inhibiting activity on cecum cancer cells.

Description

The application of Houttuynoid B in preparation treatment ileocecum cancer drug
Technical field
The present invention relates to the new purposes of compound H outtuynoid B, relate in particular to the application of Houttuynoid B in the anti-ileocecum cancer drug of preparation.
Technical background
Cancer is to one of disease of human life's health hazard maximum, and annual have a large amount of people to die from cancer.The research and development of cancer therapy drug are the focuses of study of pharmacy always.Having 74% to be the natural product or derivatives thereof in the antitumor drug, is exactly the present reasonable antitumor drug of effect clinically such as paclitaxel and derivant thereof.Therefore, searching anticancer compound or lead compound have great importance from natural product.
The compound H outtuynoid B that the present invention relates to is one and delivered (Chen in 2012, S. D. et al., 2012. Houttuynoid B_E, Anti-Herpes Simplex Virus Active Flavonoids with Novel Skeletons from Houttuynia cordata. Organic Letters 14 (7), 1772 – 1775.) New skeleton compound, this chemical compound has brand-new framework types, present purposes only relates to anti-herpes simplex virus activity (Chen, S. D. et al., 2012. Houttuynoid B_E, Anti-Herpes Simplex Virus Active Flavonoids with Novel Skeletons from Houttuynia cordata. Organic Letters 14 (7), 1772 – 1775.), belong to open first for the purposes of the Houttuynoid B that the present invention relates in preparation treatment ileocecum cancer drug, because framework types belongs to brand-new framework types, and its inhibition for the ileocecum cancerous cell is active unexpectedly strong, there is not the possibility that is provided any enlightenment by other chemical compounds, possess outstanding substantive distinguishing features, the control that is used for simultaneously the ileocecum cancer obviously has significant progress.
Summary of the invention
The invention provides the application of compound H outtuynoid B in the preparation antitumor drug.
The present invention adopts following technical scheme: the application of Houttuynoid B in the anti-ileocecum cancer drug of preparation, and the structural formula of Houttuynoid B is shown in formula I:
Figure BDA0000231838801
The present invention finds that by external MTT anti-tumor activity evaluation Houttuynoid B also has significant inhibitory action to the growth of human ileocecal carcinoma cell strain HCT-8, suppresses the IC of this 1 strain Growth of Cells 50Value is respectively 0.22 ± 0.07 μ M.Therefore, Houttuynoid B can for the preparation of anti-ileocecum cancer drug, have good development prospect.
The purposes of the Houttuynoid B that the present invention relates in preparation treatment ileocecum cancer drug belongs to open first, because framework types belongs to brand-new framework types, and its inhibition for the ileocecum cancerous cell is active unexpectedly strong, there is not the possibility that is provided any enlightenment by other chemical compounds, possess outstanding substantive distinguishing features, the control that is used for simultaneously the ileocecum cancer obviously has significant progress.
The present invention is further detailed explanation by the following examples, but protection scope of the present invention is not subjected to any restriction of specific embodiment, but limited by claim.
The specific embodiment
The preparation method of compound H outtuynoid B involved in the present invention is referring to document (Chen, S. D. et al., 2012. Houttuynoid B_E, Anti-Herpes Simplex Virus Active Flavonoids with Novel Skeletons from Houttuynia cordata. Organic Letters 14 (7), 1772 – 1775.).
The present invention is further detailed explanation by the following examples, but protection scope of the present invention is not subjected to any restriction of specific embodiment, but limited by claim.
Embodiment 1: the preparation of compound H outtuynoid B tablet involved in the present invention:
Get 20 and digest compound Houttuynoid B, add conventional adjuvant 180 grams of preparation tablet, mixing, conventional tablet machine are made 1000.
Embodiment 2: the preparation of compound H outtuynoid B capsule involved in the present invention:
Get 20 and digest compound Houttuynoid B, add conventional adjuvant such as starch 180 grams of preparation capsule, mixing is encapsulatedly made 1000.
Further specify its pharmaceutically active below by pharmacodynamic experiment.
Experimental example: adopt mtt assay assessing compound Houttuynoid B to the growth inhibited effect of human ileocecal carcinoma cell strain
1. method: the cell that is in the growth logarithmic (log) phase: human ileocecal carcinoma cell strain HCT-8(buys from Chinese Academy of Sciences's cell bank) with 1.5 * 10 4The concentration kind is in 96 orifice plates.Suck original culture medium after cell culture 24 h are adherent.Test is divided into blank group, drug treating group.Blank group is changed 1640 culture medium that contain 10% hyclone; It is 100 μ M that the replacing of drug treating group contains concentration, 50 μ M, 10 μ M, 1 μ M, 0.1 μ M, 0.01 μ M, 0.001 μ M, the culture medium of the Houttuynoid B of 0.0001 μ M and 0.00001 μ M.After cultivating 48 h, add the MTT of concentration 5mg/mL, continue to be put in CO 2Incubator is cultivated 4 h, then suck 100 μ L supernatants along culture fluid top, add 100 μ L DMSO, 10 min are placed in the dark place, utilize microplate reader (Sunrise company product) to measure light absorption value (wavelength 570nm), and according to light absorption value calculating cell survival situation, 6 repeating holes are established in each processing.Cell survival rate (%)=Δ OD Drug treating/ Δ OD Blank* 100.
2. result: Houttuynoid B has significant inhibitory action to the growth of human ileocecal carcinoma cell strain HCT-8.This chemical compound suppresses the IC of human ileocecal carcinoma cell strain HCT-8 growth 50Value is respectively: 0.22 ± 0.07 μ M.
Shown that by above-described embodiment Houttuynoid B of the present invention has good inhibitory action to the growth of human ileocecal carcinoma cell strain HCT-8.Prove that thus it is active that Houttuynoid B of the present invention has anti-ileocecum cancer, can be for the preparation of anti-ileocecum cancer drug.

Claims (1)

1.Houttuynoid the application of B in preparation treatment ileocecum cancer drug, described compound H outtuynoid B structure as Formula IShown in:
Formula I.
CN 201210419692 2012-10-27 2012-10-27 Application of Houttuynoid B in medicament for treating cecum cancer Expired - Fee Related CN102872149B (en)

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